LONDON, UK I September 13, 2013 I GlaxoSmithKline plc (LSE:GSK) and Genmab A/S (OMX: GEN) announced today that the US Food and Drug Administration (FDA) has granted Breakthrough Therapy designation for Arzerra® (ofatumumab) in combination with chlorambucil for the treatment of patients with chronic lymphocytic leukaemia (CLL) who have not received prior treatment and are inappropriate for fludarabine-based therapy. Ofatumumab is not approved or licensed anywhere in the world for use in this treatment setting. Breakthrough Therapy Designation is the newest of the FDA’s programs aimed at accelerating the development and review times of drugs for serious or life-threatening conditions.
CLL is the most common form of leukaemia in adults. Based on estimates by the American Cancer Society, CLL will account for more than 15,680 new cases and more than 4,580 deaths in the United States of America alone in 2013. At present, no curative chemotherapy is available.
The Breakthrough Therapy designation was based on the results from an international, multicentre, randomised Phase III clinical trial in more than 400 patients with previously untreated CLL. Headline results from this trial were announced in May 2013 and the full study results have been submitted for presentation at the 2013 American Society of Hematology Annual Meeting in December.
“We are exceedingly proud to receive the Breakthrough Therapy designation, the second this year for GSK. This FDA programme is intended to expedite not just the development but also the review of drugs for serious or life threatening conditions.” said Dr. Kathy Rouan, Vice President and Head of Biopharmaceutical Development, GlaxoSmithKline “We are actively working on our submission and look forward to the enhanced regulatory interaction allowed for Breakthrough Therapies.”
“Both of Genmab’s lead products, ofatumumab and daratumumab, have now been granted Breakthrough Therapy Designations from the FDA. This designation for ofatumumab reflects Genmab’s mission to create differentiated products aimed at improving the lives of patients suffering from debilitating diseases and for whom existing treatments are inadequate,” said Jan van de Winkel, Ph.D., Chief Executive Officer of Genmab.
About Breakthrough Therapy Designation
The Breakthrough Therapy designation was enacted as part of the 2012 FDA Safety and Innovation Act (FDASIA) and is intended to expedite development and review of drugs to treat serious or life-threatening medical conditions when preliminary clinical evidence demonstrates that the drug may have substantial improvement on at least one clinically significant endpoint over available therapies. Breakthrough Therapy designation includes all the features of the Fast Track designation, as well as more intensive guidance from the FDA on a drug’s clinical development program.
About ofatumumab
Ofatumumab is a human monoclonal antibody which targets an epitope on the CD20 molecule encompassing parts of the small and large extracellular loops[i]. Ofatumumab is being developed under a co-development and commercialisation agreement between Genmab and GSK. For Full US Prescribing Information for the approved indication, please visit: us.gsk.com/html/medicines/index.html and visit health.gsk.com for the EU SPC for the approved indication.
GlaxoSmithKline – one of the world’s leading research-based pharmaceutical and healthcare companies – is committed to improving the quality of human life by enabling people to do more, feel better and live longer. For further information please visit www.gsk.com.
SOURCE: GlaxoSmithKline
Post Views: 76
LONDON, UK I September 13, 2013 I GlaxoSmithKline plc (LSE:GSK) and Genmab A/S (OMX: GEN) announced today that the US Food and Drug Administration (FDA) has granted Breakthrough Therapy designation for Arzerra® (ofatumumab) in combination with chlorambucil for the treatment of patients with chronic lymphocytic leukaemia (CLL) who have not received prior treatment and are inappropriate for fludarabine-based therapy. Ofatumumab is not approved or licensed anywhere in the world for use in this treatment setting. Breakthrough Therapy Designation is the newest of the FDA’s programs aimed at accelerating the development and review times of drugs for serious or life-threatening conditions.
CLL is the most common form of leukaemia in adults. Based on estimates by the American Cancer Society, CLL will account for more than 15,680 new cases and more than 4,580 deaths in the United States of America alone in 2013. At present, no curative chemotherapy is available.
The Breakthrough Therapy designation was based on the results from an international, multicentre, randomised Phase III clinical trial in more than 400 patients with previously untreated CLL. Headline results from this trial were announced in May 2013 and the full study results have been submitted for presentation at the 2013 American Society of Hematology Annual Meeting in December.
“We are exceedingly proud to receive the Breakthrough Therapy designation, the second this year for GSK. This FDA programme is intended to expedite not just the development but also the review of drugs for serious or life threatening conditions.” said Dr. Kathy Rouan, Vice President and Head of Biopharmaceutical Development, GlaxoSmithKline “We are actively working on our submission and look forward to the enhanced regulatory interaction allowed for Breakthrough Therapies.”
“Both of Genmab’s lead products, ofatumumab and daratumumab, have now been granted Breakthrough Therapy Designations from the FDA. This designation for ofatumumab reflects Genmab’s mission to create differentiated products aimed at improving the lives of patients suffering from debilitating diseases and for whom existing treatments are inadequate,” said Jan van de Winkel, Ph.D., Chief Executive Officer of Genmab.
About Breakthrough Therapy Designation
The Breakthrough Therapy designation was enacted as part of the 2012 FDA Safety and Innovation Act (FDASIA) and is intended to expedite development and review of drugs to treat serious or life-threatening medical conditions when preliminary clinical evidence demonstrates that the drug may have substantial improvement on at least one clinically significant endpoint over available therapies. Breakthrough Therapy designation includes all the features of the Fast Track designation, as well as more intensive guidance from the FDA on a drug’s clinical development program.
About ofatumumab
Ofatumumab is a human monoclonal antibody which targets an epitope on the CD20 molecule encompassing parts of the small and large extracellular loops[i]. Ofatumumab is being developed under a co-development and commercialisation agreement between Genmab and GSK. For Full US Prescribing Information for the approved indication, please visit: us.gsk.com/html/medicines/index.html and visit health.gsk.com for the EU SPC for the approved indication.
GlaxoSmithKline – one of the world’s leading research-based pharmaceutical and healthcare companies – is committed to improving the quality of human life by enabling people to do more, feel better and live longer. For further information please visit www.gsk.com.
SOURCE: GlaxoSmithKline
Post Views: 76
